Work Flexibility: Hybrid
Position summary: This role will provide functional and technical support to corporate clinical team in executing projects to support global clinical strategy.
Key Responsibilities:
• Project management for enterprise level tools or systems. Support divisional user needs as administrator/superuser/SME for existing clinical systems); Responsible for following in case of enterprise systems/tools:
o Creation of procedures and corporate documents
o Centralized Communication
o Knowledge Base Development
o Divisions On-boarding & User Access management
o Training & Development Planning
o Change Management in Azure Devops
• Provide support to clinical global process owner (GPO) in coordinating with functional partners: IT, Indirect Procurement, Legal, Clinical Heads
• Provide support to explore enterprise opportunities– understand vendor landscape, guide selection of tools and systems, provide decision framework for evaluation.
• Provide assistance when divisions need replacement or new clinical tool.
• Support creation of global clinical metrics e.g. clinical trial dashboard, CER matrix etc.
• Provide support in writing corporate clinical procedures, work-instructions etc. as needed.
• Bridge gaps when new regulatory systems with clinical requirements go live (e.g., EUDAMED)
• Help clinical GPO in setting clinical policy at the corporate level on a variety of topics and projects.
• Manage global newsletter and global clinical trial dashboard in SharePoint or power BI
• Represent the corporate perspective while building and maintaining strong collaborative relationships with Stryker divisions.
• Assist in management of various clinical forums including SCAN (Stryker Clinical Affairs Network) and EUMDR clinical monthly meetings.
Education & Work Experience:
• Bachelor's level degree or equivalent in science or health care field with at least 2 years of relevant industry experience.
• Preferred experience as clinical research professional or data management
• Proficiency and knowledge in computer applications e.g. excel, power BI, SharePoint etc.
• Familiarity with Good Clinical Practices (GCPs) and regulatory and compliance guidelines for clinical trials, CTMS, EDC, eTMF etc.
• Excellent verbal and written communication skills
• Well-developed interpersonal skills and the ability to work well independently as well as with colleagues and customers.
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